跳至主要内容
临床试验/NCT01959100
NCT01959100Unknown3 期

Evaluation of the Efficacy of Azithromycin to Prevent Bronchiolitis Obliterans Syndrome After Allogeneic Hematopoietic Stem Cell Transplantation

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 480 人开始时间: 2014年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
480
试验地点
1
主要终点
Airflow decline (AFD)-free survival

研究概览

简要总结

The occurrence of bronchiolitis obliterans syndrome (SBO) after allogeneic hematopoietic stem cell transplantation (HSCT) is considered to be a chronic pulmonary graft versus host disease (GVHD) that is associated with significant mortality and morbidity. The reported incidence of SBO varies from 6 to 26% of allogeneic HSC recipients and is usually diagnosed within 2 years after transplantation. The diagnosis of SBO relies on the occurrence of a new airflow obstruction identified during pulmonary function testing, and the definition differs between studies. Currently, no curative immunosuppressive treatment is available, and recent data suggest that the use of these treatments, especially corticosteroids, should be limited because of their toxicity. The impairment of lung function parameters is likely caused by fibrous small airway lesions. Few data on the pathogenesis of SBO after allogeneic HSCT are available. Several hypotheses are based on the occurrence of SBO during chronic graft rejection after lung transplantation, which shares many clinical and histopathological similarities with SBO after allogeneic HSCT. One hypothesis is that the first step leading to SBO is lung epithelium injury. SBO is then identified as an alloimmune reaction with only one clearly identified risk factor: extrathoracic chronic GVHD. Due to their anti-inflammatory and immunomodulatory properties, recent data suggest that low-dose macrolides may be effective at preventing SBO after lung transplants. This well-tolerated treatment may be useful for preventing SBO after allogeneic HSCT.

The objective of this Phase 3 multicentre randomized, double-blinded, clinical trial is to evaluate the efficacy of azithromycin in preventing BO syndrome after allogeneic HSCT in patients with malignant hematological diseases.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients> 16 years old
  • Experimenting an allogeneic HSCT for a hematologic malignancy
  • Pre-transplantation Pulmonary Function Testing
  • With written informed consent

排除标准

  • Allergy or Intolerance to azithromycin, macrolides or ketolide or excipient
  • Prolonged corrected QT (QTc) interval (>450 msec)
  • Taking medications that prolong the QTc interval (Cisapride, ergotamine, dyhydroergotamine)
  • Taking ergotamine and dyhydroergotamine due to the risk of ergotism
  • Family history of a prolonged QTc interval.
  • History of congestive heart failure
  • Taking colchicine Severe liver insufficiency • History of infection due to atypical mycobacteria

研究组 & 干预措施

Azithromycine

Experimental

250 mg x 3/week during a meal for a period of 2 years

干预措施: Azithromycin (Drug)

Placebo

Placebo Comparator

250 mg x 3/week during a meal for a period of 2 years.

干预措施: Placebo (Drug)

结局指标

主要结局

Airflow decline (AFD)-free survival

时间窗: 2 year after allogeneic HSCT

Defined on the criteria from Chien JW et al (Am J Resp Crit Care Med 2003;168:208-14) by an annualized decline of percent predicted forced expiratory volume in 1 second (FEV1) of more than 5%

次要结局

  • Overall survival(within 2 years of inclusion)
  • Occurrence of late-onset pulmonary non-infectious complications (=bronchiolitis obliterans syndrome, SBO)(within 2 years after inclusion)
  • Occurrence of acute and chronic extra-thoracic graft versus host disease (GVHD)(within 2 years after inclusion)
  • Cumulative incidence of hematological relapse(within the 2 years after inclusion)
  • Quality of life(within 2 years after inclusion)
  • Cumulative dose of steroids treatment(within the 2 years after inclusion)
  • Variation of pulmonary function testing parameters(within 2 years after inclusion)
  • Tolerance(within 2 years of inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验